Systems and methods of diagnosing and characterizing infections

ABSTRACT

Embodiments of the invention include methods of identifying microorganisms and/or diagnosing infections in subjects cause by microorganisms. Embodiments of the invention may also include further characterizing (e.g., determining the presence of one or more antibiotic resistance markers) the microorganisms and determining a strain identity of the microorganisms.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 15/773,270, filed on May 3, 2018 (published as US20190024139), which is the U.S. National Stage of International Application No. PCT/US2016/060369, filed on Nov. 3, 2016, which claims priority to and the benefit of U.S. Provisional Application Ser. No. 62/250,565, filed on Nov. 4, 2015, the contents of each of which are hereby incorporated by reference in their entireties.

INCORPORATION-BY-REFERENCE OF MATERIAL ELECTRONICALLY FILED

Incorporated by reference in its entirety herein is a computer-readable nucleotide/amino acid sequence listing submitted concurrently herewith and identified as follows: One 77,824 byte ASCII (text) file named “91482_196_Sequence_Listing” created on Oct. 29, 2016.

FIELD OF INVENTION

The present invention is generally related to systems and methods of sequencing biological molecules for determinations regarding the presence and/or absence of infectious agents, and particularly related to systems and methods for the diagnosis of infections and determination of the presence of antimicrobial-resistance markers using nucleic-acid sequencing (e.g., amplicon-based sequencing).

BACKGROUND OF THE INVENTION

Once highly treatable, common bacterial infections are becoming increasingly more difficult to characterize and manage. Gram-negative infections, including Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, Enterobacter species and Escherichia coli and Gram-positive infections, including Staphylococcus aureus, are all considered high-priority target pathogens for which new therapeutics are urgently needed. These are the components of the widely recognized ESKAPE pathogens, which have become a focal point for the development of new antibiotics. The lack of new drugs makes it critical that clinicians receive rapid and informative data on their patients' infections and their likely response to therapy. This clinical and public health crisis is coming at a time when we have greater scientific understanding of the mechanisms of resistance and better access to molecular technology to detect and characterize those mechanisms than ever before; however, the barriers between genomic research and the clinical lab also remains large and therefore the separation between genotype and phenotype remains largely un-bridged.

Some of these ESKAPE pathogens (e.g., K. pneumoniae, A. baumannii, P. aeruginosa, Enterobacter spp. and ExPEC E. coli) are all widely distributed Gram-negative bacteria demonstrating high levels of multi-drug resistance, including resistance to carbapenems and other last-line drugs. While similar in many respects, including all being primary causes of healthcare-associated infections (HAI), individually, these organisms present many unique problems to clinical medicine and public health. P. aeruginosa is a major cause of pneumonia in cystic fibrosis patients and outbreaks in neonatal intensive care units, and is frequently shown to colonize water networks in hospitals. Its high rates of intrinsic resistance frequently confound clinical susceptibility testing. A. baumannii is responsible for up to 80% of all intensive care unit (ICU) bloodstream infections; its high-rate of transmission in the healthcare setting can be attributed to high desiccation tolerance, enabling it to survive for long periods on fomites. Extra-intestinal Pathogenic E. coli (ExPEC) has become a global cause of antimicrobial resistance (AR) bacteremia and urinary tract infections, particularly specific strains, such as the well-studied ST131 strain. Enterobacter has been seen to have comparable prevalence of ESBLs and other plasmid-mediated resistance as Klebsiella and E. coli. In addition, at least some of the aforementioned pathogens have developed resistance to multiple antibiotics typically through several different mechanisms. The mechanisms for resistance are variable, can occur in combinations and in some cases are synergistic.

The rapid depletion of available antibiotics combined with an even more rapid increase in bacterial mechanisms of multi-drug resistance is a call to action for molecular researchers, medical and public health officials and the biomedical industry to join forces to develop and translate more informative diagnostic tools for the clinician, to better characterize and respond to AR in bacterial infections. While bacterial culturing may remain the gold standard for diagnosis and characterizing resistance, standard culturing processes are time consuming, potentially hazardous, and require specific microbiological skills and facilities.

In addition, antibiotic susceptibility analysis techniques may vary for different species, as there is no single approach that can be used to rapidly diagnose and characterize infections with all target agents. Clearly a new approach is required—the detection of established and emerging multi-drug resistant bacteria directly from clinical specimens demands a sensitive and comprehensive diagnostic approach that is capable of rapidly identifying trace amounts of genotypic targets in human samples and using that information to develop phenotypic profiles. The scientific and clinical research community now has more knowledge and cutting edge technology than ever before, allowing them to address this health crisis with such an approach.

Given these public-health issues, there is a demonstrated need to develop a novel, multiplexed, targeted sequence analysis system for the detection and characterization of AR markers in critical ESKAPE bacteria, typically associated with HAIs, directly from clinical samples. As described herein, the inventors have developed an approach that is capable of identifying all known classes of AR mechanisms, including mutations, SNPs, mobile elements, gene amplification, and expression modulation.

DETAILED DESCRIPTION

As used herein, the verb “comprise” as is used in this description and in the claims and its conjugations are used in its non-limiting sense to mean that items following the word are included, but items not specifically mentioned are not excluded. Plural encompasses singular and vice versa; e.g., the singular forms “a,” “an,” and “the” include plural referents unless expressly and unequivocally limited to one referent.

Some embodiments of the invention provide systems and methods for diagnosing and/or identifying infectious organisms and thereafter making one or more genotypic determinations. Moreover, in addition to the diagnostic and genotypic capabilities of the instant invention, some embodiments may also provide methodologies of making genetic/typing determinations of the infectious organisms to provide those of ordinary skill in the art with epidemiological information about the infectious organisms (e.g., strain type). In addition, some embodiments of the invention can be employed with samples that do not require isolation and culturing of the infectious organisms (i.e., embodiments include the capability to directly analyze samples from a patient).

Some embodiments of the invention may provide methods of (i) diagnosing and/or identifying an infectious organism; (ii) determining the presence of one or more antibiotic resistance targets of the infectious organism; and/or (iii) determining a strain identity of the infectious organism. In some aspects, these three steps of some embodiments of the invention may be performed substantially or completely simultaneously, or, in other aspects, may be performed sequentially (e.g., in any sequence). Moreover, in some embodiments, one or more of these three steps may be omitted. For example, in some embodiments, the first two steps may be performed according to some aspects of the invention and the user may omit the third step in the event that the user does not desire strain information about the infectious organism. In other embodiments, one or more of the first and/or second steps recited above may be omitted.

With respect to the three steps/methodologies, some or all of these steps may include an analysis of one or more markers at each step. For example, pre-selected markers can be used to make determinations regarding the presence and/or absence of one or more infectious microorganisms (e.g., ESKAPE pathogens). In particular, a series of pre-selected markers may be chosen to provide relevant differential information regarding the identification. For example, makers can be selected that are specific for a plurality of potentially pathogenic microorganisms so that presence or absence of certain markers provides highly specific relevant information. Moreover, the same and/or different pre-selected markers can be used to make predictions about a phenotype of the infectious microorganisms. In some embodiments, as described in greater detail below, the phenotypic predictions can be generally or specifically directed to determining the presence of one or more AR markers. In addition, some of the same and/or different pre-selected markers as recited above can be used to provide users with information regarding a strain identity of the infectious microorganism.

As described in greater detail herein, some embodiments of the invention may include amplicon-based sequencing of the one or more markers to make the aforementioned determinations. Some embodiments of the invention include systems and methods of preparing samples for one or more downstream processes that can be used for assessing one or more markers for any of the previously mentioned purposes. Some embodiments of the invention may comprise a universal indexing sequencing strategy for use in downstream sequencing platform processes. By way of example only, some embodiments of the invention comprise a universal indexing sequencing strategy that can be used to amplify multiple genomic regions (e.g., markers, as described below) from a DNA sample simultaneously in a single reaction for the sequencing of one or more amplicons. One or more embodiments of the invention can be used with any desired sequencing platform, such as the ILLUMINA® Next Generation Sequencing (e.g., MiSEQ) platform, Life Technologies' Ion Torrent System, or any other sequencing system now known or developed in the future.

Some embodiments may be configured to enable relatively simple, rapid (e.g., microorganism-culture independent), inexpensive, and efficient preparation of samples for use on, in, and/or with downstream sequencing platforms. For example, some embodiments may use a sequence coupled to one or more oligonucleotides/primers (as used herein, oligonucleotides and primers are used interchangeably). More specifically, one or more amplicons per sample can be generated using a hybrid oligonucleotide that is designed for amplification of a marker and incorporation of at least one universal tail sequence into the resulting amplicon. As a result, additional steps that may be conventionally required to prepare samples for sequencing can be limited or removed entirely. Further information regarding the universal tail, amplicon-based sequencing strategy can be found in PCT/US2014/064890, which is hereby incorporated by reference in its entirety for all purposes.

In some embodiments, the methodology may include performing downstream sequencing on one or more amplicons. For example, in order to minimize and/or eliminate the need for cultures of microorganisms or large inputs of nucleic acids, methodologies of the instant invention may include an initial PCR step to create amplicons that correspond to the one or more pre-selected markers. As such, some embodiments require only limited amounts of starting material are necessary and the starting material need not be of high quality (e.g., genomic DNA, crude DNA extracts, single stranded DNA, RNA, cDNA, etc.). In contrast, many conventional sample preparation systems may require relatively large amounts of starting material of relatively high quality, which can limit the use of some conventional systems.

Some embodiments of the invention can be used for and/or in complement with high-throughput amplicon sequencing of markers, which can be very useful for a variety of molecular genetic genotyping/predicted-phenotyping applications, including clinical sample analysis. For example, use of the systems and methods of the invention can be employed with sequencing platforms to provide rapid, high-yield sequence data, which can enable the sequencing of multiple markers/amplicons from many samples in a relatively short period of time. Specifically, in some embodiments, amplicons can be selected and PCR reactions can be designed to provide information that can be used to make clinically relevant determinations after sequencing of the amplicons.

Overall, embodiments of the invention may generally include systems and methods that provide multiplexed marker/sequence amplification, sequencing, and analysis for the identification/detection and characterization of AR markers in critical ESKAPE pathogens and HAI-related pathogens from culture-independent samples. In other words, embodiments of the invention provide diagnostic methodologies with the ability to provide phenotypic and predicted-genotypic information without the need for separately culturing a sample from a subject. In conventional diagnostic procedures, the need for culturing can add time and complexity, which is avoided by the instantly recited invention.

In some preferred aspects, the methodology may include creating a series of oligonucleotides designed to provide multiplexed amplification of one or more markers to produce the desired amplicons. In particular, the one or more markers and amplicons thereof can be selected/amplified to provide users with clinically relevant information related to identification of one or more potentially infectious microorganisms and phenotypic and genotypic information about the microorganisms (e.g., AR status and strain identity). After production of the amplicons (e.g., via PCR amplification), which may include the universal tail sequences, as detailed above and below, the method may include processing the resulting amplicons for downstream sequencing and thereafter sequencing the processed amplicons. After processing and analysis of the resulting sequencing data, one of skill in the art can make any necessary determinations regarding the identification of one or more microorganisms that may have been contained within the sample and predicted-phenotypic and/or genotypic information revealed.

Generally, some embodiments of the present invention can be used to detect, identify, assess, sequence, or otherwise evaluate a marker. A marker may be any molecular structure produced by a cell, expressed inside the cell, accessible on the cell surface, or secreted by the cell. A marker may be any protein, carbohydrate, fatty acid, nucleic add, catalytic site, or any combination of these such as an enzyme, glycoprotein, cell membrane, virus, a particular cell, or other uni- or multimolecular structure. A marker may be represented by a sequence of a nucleic acid or any other molecules derived from the nucleic acid. Examples of such nucleic acids include miRNA, tRNA, siRNA, mRNA, cDNA, genomic DNA sequences, single-stranded DNA, or complementary sequences thereof. Alternatively, a marker may be represented by a protein sequence. The concept of a marker is not limited to the exact nucleic acid sequence or protein sequence or products thereof, rather it encompasses all molecules that may be detected by a method of assessing the marker. Without being limited by the theory, the detection, identification, assessment, sequencing, or any other evaluation of the marker may encompass an assessment of a change in copy number (e.g., copy number of a gene or other forms of nucleic acid) or in the detection of one or more translocations. Moreover, in some embodiments, the marker may be relevant to a particular phenotype or genotype. By way of example only; in some embodiments, the marker may be related to phenotypes including antibiotic resistance, virulence, or any other phenotype.

Therefore; examples of molecules encompassed by a marker represented by a particular sequence further include alleles of the gene used as a marker. An allele includes any form of a particular nucleic acid that may be recognized as a form of the particular nucleic acid on account of its location, sequence, or any other characteristic that may identify it as being a form of the particular gene. Alleles include but need not be limited to forms of a gene that include point mutations, silent mutations, deletions, frameshift mutations, single nucleotide polymorphisms (SNPs), inversions, translocations, heterochromatic insertions; and differentially methylated sequences relative to a reference gene, whether alone or in combination. An allele of a gene may or may not produce a functional protein; may produce a protein with altered function; localization, stability, dimerization, or protein-protein interaction; may have overexpression, underexpression or no expression; may have altered temporal or spatial expression specificity; or may have altered copy number (e.g., greater or less numbers of copies of the allele). An allele may also be called a mutation or a mutant. An allele may be compared to another allele that may be termed a wild type form of an allele. In some cases, the wild type allele is more common than the mutant.

In some aspects, the markers may include one or more sets of amplifiable nucleic acids that can provide diagnostic information about the microorganisms. For example, the markers may include amplifiable nucleic acid sequences that can be used to assess the presence and/or absence of one or more microorganism that may have the potential to cause a diseased state in the subject. In some embodiments, the markers may include amplifiable nucleic acid sequences that can be used to identify one or more of the following exemplary microorganisms: Klebsiella pneumoniae, Serratia marcescens, Proteus mirabills, Providencia alcalifaciens, Providencia stuartii. Enterococcus faecalis, Enterococcus faeciurn, Klebsiella oxytoca, Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli. Acinetobacter baumanii, Acinetobacter calcoaceticus (including the Acb complex), Streptococcus pneumoniae, Streptococcus agalactiae, Enterobacter cloacal, Enterobacter aerogenes, Streptococcus pyogenes, Streptococcus dysgalactia, and Streptococcus equi. In some embodiments, the methods may include the use of one or more than one marker per microorganism. Moreover, in some embodiments, one or more of the microorganisms may not be considered pathogenic to certain subjects, but the methodology employed herein can still rely on detection of pathogenic and non-pathogenic microorganisms for differential diagnoses/diagnostics. In some embodiments, the oligonucleotides (with or without the universal tail sequences detailed herein) listed in Table 1 can be used with embodiments of the invention to amplify one or more markers from the microorganisms to provide diagnostic/identification information to the user.

Moreover, in some embodiments, one or more the markers associated with the plurality of microorganisms can be amplified in a multiplex manner. For example, in some aspects, nucleic acids can be obtained from the sample and the oligonucleotides used to amplify one or more of the markers used to identify/diagnose can be added to a single mixture to produce a plurality of amplicons in a single reaction mixture. In other aspects, the oligonucleotides can be added to multiple mixtures to provide for the creation of multiple amplicons in multiple mixtures.

In some aspects, the markers may include one or more sets of amplifiable nucleic acids that can provide characterization information about the microorganisms. For example, the markers may include amplifiable nucleic acid sequences that can be used to assess the presence and/or absence of one or more antibiotic resistance (AR) mechanisms within the microorganisms. In some embodiments, the markers may include amplifiable nucleic add sequences that can be used to identify the presence of one or more of the following AR markers: bla_(tem), bla_(shv), bla_(rob), bla_(oxo), blaZ, aadB, aacC1, aacC2, aacC3, aac6′-IIa, aacA4, aad(6′), vanA, vanB, vanC, msrA, sarA, aac(6′) aph(2″), vat, vga, ermA, ermB, ermC, mecA, int, sul, mecA, aac2ia, aac2ib, aac2ic, aac2id, aac2i, aac3ia, aac3iia, aac3iib, aac3iii, aac3iv, aac3ix, aac3vi, aac3viii, aac3vii, aac3x, aac6i, aac6ia, aac6ib, aac6ic, aac6ie, aac6if, aac6ig, aac6iia, aac6iib, aad9, aad9ib, aadd, acra, acrb, adea, adeb, adec, amra, amrb, ant2ia, ant2ib, ant3ia, ant4iia, ant6ia, aph33ia, aph33ib, aph3ia, aph3ib, aph3ic, aph3iiia, aph3iva, aph3va, aph3vb, aph3via, aph3viia, aph4ib, aph6ia, aph6ib, aph6ic, aph6id, arna, baca, bcra, bcrc, bl1_acc, bl1_ampc, bl1_asba, bl1_ceps, bl1_cmy2, bl1_ec, bl1_fox, bl1_mox, bl1_och, bl1_pao, bl1_pse, bl1_sm, bl2a_1, bl2a_exo, bl2a_iii2, bl2a_iii, bl2a_kcc, bl2a_nps, bl2a_okp, bl2a_pc, bl2be_ctxm, bl2be_oxy1, bl2be_per, bl2be_shv2, bl2b_rob, bl2b_tem1, bl2b_tem2, bl2b_tem, bl2b_tle, bl2b_ula, bl2c_bro, bl2c_pse1, bl2c_pse3, bl2d_lcr1, bl2d_moxa, bl2d_oxa10, bl2d_oxa1, bl2d_oxa2, bl2d_oxa5, bl2d_oxa9, bl2d_r39, bl2e_cbla, bl2e_cepa, bl2e_cfxa, bl2e_fpm, bl2e_y56, bl2f_nmca, bl2f_sme1, bl2_ges, bl2_kpc, bl2_len, bi2_veb, bl3_ccra, bl3_cit, bl3_cpha, bl3_gim, bl3_imp, bl3_I, bl3_shw, bl3_sim, bl3_vim, ble, bit, bmr, cara, cata10, cata11, cata12, cata13, cata14, cata15, cata16, cata1, cata2, cata3, cata4, cata5, cata6, cata7, cata8, cata9, catb1, catb2, catb3, catb4, catb5, ceoa, ceob, cml_e1, cml_e2, cml_e3, cml_e4, cml_e5, cml_e6, cml_e7, cml_e8, dfra10, dfra12, dfra13, dfra14, dfra15, dfra16, dfra17, dfra19, dfra1, dfra20, dfra21, dfra22, dfra23, dfra24, dfra25, dfra25, dfra25, dfra26, dfra5, dfra7, dfrb1, dfrb2, dfrb3, dfrb6, emea, emrd, emre, erea, ereb, erma, ermb, emnc, ermd, erme, ermf, ermg, ermh, ermn, ermo, ermq, ermr, ems, ermt, ermu, ermv, ermw, ermx, ermy, fosa, fosb, fosc, fosx, fusb, fush, ksga, lmra, lmrb, lnua, lnub, lsa, maca, macb, mdte, mdtf, mdtg, mdth, mdtk, mdtl, mdtm, mdtn, mdto, mdtp, meca, mecr1, mefa, mepa, mexa, mexb, mexc, mexd, mexe, mexf, mexh, mexi, mexw, mexx, mexy, mfpa, mpha, mphb, mphc, msra, norm, oleb, opcm, opra, oprd, oprj, oprm, opm, otra, otrb, pbpla, pbplb, pbp2b, pbp2, pbp2x, pmra, qac, qaca, qacb, qnra, qnrb, qnrs, rosa, rosb, smea, smeb, smec, smed, smee, smef, srmb, sta, str, sul1, sul2, sul3, tcma, tcr3, tet30, tet31, tet32, tet33, tet34, tet36, tet37, tet38, tet39, tet40, teta, tetb, tetc, tetd, tete, tetg, teth, tetj, tetk, tetl, tetm, teto, tetpa, tetpb, tet, tetq, tets, tett, tetu, tetv, tetw, text, tety, tetz, tirc, tmrb, toic, tsnr, vana, vanb, vanc, vand, vane, vang, vanha, vanhb, vanhd, vanra, vanrb, vanrc, vanrd, vanre, vanrg, vansa, vansb, vansc, vansd, vanse, vansg, vant, vante, vantg, vanug, vanwb, vanwg, vanxa, vanxb, vanxd, vanxyc, vanxye, vanxyg, vanya, vanyb; vanyd, vanyg, vanz, vats, vatb, vatc, vatd, vate; vgaa, vgab, vgba, vgbb, vph, ykkc, and ykkd.

In some specific embodiments of the methodology, the method may include an analysis of the following AR markers: blaKFC (beta lactam resistance), blaNDM (beta lactam resistance), rmtA (aminoglycoside resistance), rmtB (aminoglycoside resistance), rmtC (aminoglycoside resistance), rmtD1 and rmtD2 (aminoglycoside resistance), npmA (aminoglycoside resistance), armA (aminoglycoside resistance), gyrA (fluoroquinolone resistance), parC (fluoroquinolone resistance), qnrA (fluoroquinolone resistance), qnrC (fluoroquinolone resistance), qnrD (fluoroquinolone resistance), qnrS (fluoroquinolone resistance), qnrB (fluoroquinolone resistance), blaCTX-M (beta lactam resistance), dfrA markers (dihydrofolate reductase production affecting resistance to trimethoprim), dfrB markers (dihydrofolate reductase production affecting resistance to trimethoprim), sul markers (dihydropteroate synthase production affecting resistance to sulfonamides) Staphylococcus rpoB (vancomycin intermediate resistance), and known Staphylococcus AR markers, including linA, mecA, vanA, aacA, blaZ, ermA, ermC, tetK, tetM, and msrA. In some embodiments, the oligonucleotides (with or without the universal tail sequences detailed herein) listed in Table 2 can be used with embodiments of the invention to amplify one or more markers from the microorganisms to provide AR information to the user.

Moreover, in some embodiments, one or more the AR markers associated can be amplified in a multiplex manner. For example, in some aspects, nucleic acids can be obtained from the sample and the oligonucleotides used to amplify one or more of the AR markers used to identify/characterize the AR potential of the microorganisms can be added to a single mixture to produce a plurality of amplicons in a single reaction mixture. In other aspects, the oligonucleotides can be added to multiple mixtures to provide for the creation of multiple amplicons in multiple mixtures. In some aspects, amplification of the AR markers and the markers used to identify microorganisms/diagnose an infection can also occur in a multiplex manner such that some or all of the amplicons are generated in a single reaction for a particular sample. In other aspects, amplification of the AR markers and the markers used to identify microorganisms/diagnose an infection can occur in multiple reaction vessels.

In some aspects, the markers may include one or more sets of amplifiable nucleic acids that can provide strain identity information about the microorganisms. For example, the markers may include amplifiable nucleic acid sequences that can be used to assess the presence and/or absence of specific strains of microorganisms. In some embodiments, the markers may include amplifiable nucleic acid sequences that can be used to identify the presence of one or more of the following strains of microorganisms: methicillin-resistant Staphylococcus aureus (orfX junction), methicillin-resistant Staphylococcus epidermidis (orfX junction or cfr), S. aureus strain USA300, S. aureus strain CC8, S. aureus strain USA300/500, S. aureus strain Archaic Iberian, S. aureus strain True Iberian, S. aureus strain ST239, S. aureus strain CC5, Staphylococcus strains comprising the tuf gene, SCCmec typing, including the following S. aureus strains, ccrB2, mecl, IS1272J, ccrC, ccrB1, ccrB3, ccrB4, mecC2, SCCrnecIVa-J1, and sccrnecIVa. The strain identification markers may also include further S. aureus typing markers MRSA sea and MRSA seb and E. coli pathovar typing, including the following markers: Shiga toxin genes, E. coli aggR, T3SS, E coil virulence markers, E. coli and Shigella invasion antigen, E. coli enterotoxin, E. coli UPEC, E. coli H30-Rx, trpA, pabB, uidA, rfb016, and rfb025b. In some aspects, the strain identification markers may further include markers for strain identification of K, pneumoniae strains, including ST258-strain specific SNP 3576137-Y, rpoB, gapA, mdh, phosphoglucose isomerase, phoE, infB, and tonB. The markers for strain identification may also include the CG258 ID assay, a marker for Klebsiella capsule type (wzi gene of cps locus), markers for E. coli strain identification (adk, furnC, gyrB, icd, mdh, purA, and recA), markers for S. aureus strain identification (arc, aro, gip, gmk, pta, tpi, and yqi), and markers for Streptococcus pyogenes identification. Moreover, in some embodiments, one or more control nucleotide sequences can be added to any reactions to ensure proper amplification. In some embodiments, the oligonucleotides (with or without the universal tail sequences detailed herein) listed in Table 3 can be used with embodiments of the invention to amplify one or more markers from the microorganisms to provide AR information to the user. In other embodiments, the oligonucleotides (with or without the universal tail sequences detailed herein) listed in Table 9 can be used with embodiments of the invention to amplify one or more markers from the microorganisms to provide lineage identification information to the user.

Moreover, in some embodiments, one or more the strain identification markers associated can be amplified in a multiplex manner. For example, in some aspects, nucleic acids can be obtained from the sample and the oligonucleotides used to amplify one or more of the strain identification markers used to identify the strain of the microorganisms can be added to a single mixture to produce a plurality of amplicons in a single reaction mixture. In other aspects, the oligonucleotides can be added to multiple mixtures to provide for the creation of multiple amplicons in multiple mixtures. In some aspects, amplification of the strain identification markers, the AR markers, and/or the markers used to identify microorganisms/diagnose an infection can also occur in a multiplex manner such that some or all of the amplicons are generated in a single reaction for a particular sample. In other aspects, amplification of the strain identification markers, the AR markers, and/or the markers used to identify microorganisms/diagnose an infection can occur in multiple reaction vessels. Overall, as described in greater detail below, regardless of the multiplex nature of some embodiments of the invention, after amplification of the markers detailed above, the method may include processing and sequencing the resulting amplicons to provide information related to the identification, characterization, and strain identity of one or more microorganisms that may be present within the sample.

Some embodiments of the invention may comprise the use of one or more methods of amplifying a nucleic acid-based starting material (i.e., a template, including genomic DNA, crude DNA extract, single-stranded DNA, double-stranded DNA, cDNA, RNA, or any other single-stranded or double-stranded nucleic adds). Nucleic adds may be selectively and specifically amplified from a template nucleic acid contained in a sample. In some nucleic acid amplification methods, the copies are generated exponentially, Examples of nucleic acid amplification methods known in the art include: polymerase chain reaction (PCR), ligase chain reaction (LCR), self-sustained sequence replication (3SR), nucleic acid sequence based amplification (NASBA), strand displacement amplification (SDA), amplification with Qβ replicase, whole genome amplification with enzymes such as φ29, whole genome PCR, in vitro transcription with T7 RNA polymerase or any other RNA polymerase, or any other method by which copies of a desired sequence are generated.

In addition to genomic DNA, any polynucleotide sequence can be amplified with an appropriate set of primer molecules. In particular, the amplified segments created by the PCR process itself are, themselves, efficient templates for subsequent PCR amplifications.

PCR generally involves the mixing of a nucleic acid sample, two or more primers or oligonucleotides (primers and oligonucleotides are used interchangeably herein) that are designed to recognize the template DNA, a DNA polymerase, which may be a thermostable DNA polymerase such as Taq or Pfu, and deoxyribose nucleoside triphosphates (dNTP's). In some embodiments, the DNA polymerase used can comprise a high fidelity Taq polymerase such that the error rate of incorrect incorporation of dNTPs is less than one per 1,000 base pairs. Reverse transcription PCR, quantitative reverse transcription PCR, and quantitative real time reverse transcription PCR are other specific examples of PCR. In general, the reaction mixture is subjected to temperature cycles comprising a denaturation stage (typically 80-100° C.), an annealing stage with a temperature that is selected based on the melting temperature (Tm) of the primers and the degeneracy of the primers, and an extension stage (for example 40-75c C). In real-time PCR analysis, additional reagents, methods, optical detection systems, and devices known in the art are used that allow a measurement of the magnitude of fluorescence in proportion to concentration of amplified template. In such analyses, incorporation of fluorescent dye into the amplified strands may be detected or measured.

Either primers or primers along with probes allow a quantification of the amount of specific template DNA present in the initial sample. In addition, RNA may be detected by PCR analysis by first creating a DNA template from RNA through a reverse transcriptase enzyme (i.e., the creation of cDNA). The marker expression may be detected by quantitative PCR analysis facilitating genotyping analysis of the samples.

“Amplification” is a special case of nucleic acid replication involving template specificity. Amplification may be a template-specific replication or a non-template-specific replication (i.e., replication may be specific template-dependent or not). Template specificity is here distinguished from fidelity of replication (synthesis of the proper polynucleotide sequence) and nucleotide (ribo- or deoxyribo-) specificity. Template specificity is frequently described in terms of “target” specificity. Target sequences are “targets” in the sense that they are sought to be sorted out from other nucleic acid. Amplification techniques have been designed primarily for this sorting out. The amplification process may result in the production of one or more amplicons.

The term “template” refers to nucleic acid originating from a sample that is analyzed for the presence of one or more markers. In contrast, “background template” or “control” is used in reference to nucleic acid other than sample template that may or may not be present in a sample. Background template is most often inadvertent. It may be the result of carryover, or it may be due to the presence of nucleic acid contaminants sought to be purified out of the sample. For example, nucleic acids from organisms other than those to be detected may be present as background in a test sample.

In addition to primers and probes, template specificity is also achieved in some amplification techniques by the choice of enzyme. Amplification enzymes are enzymes that, under the conditions in which they are used, will process only specific sequences of nucleic acid in a heterogeneous mixture of nucleic acid. Other nucleic acid sequences will not be replicated by this amplification enzyme. Similarly, in the case of T7 RNA polymerase, this amplification enzyme has a stringent specificity for its own promoters (Chamberlin et al. (1970) Nature (228):227). In the case of T4 DNA ligase, the enzyme will not ligate the two oligonucleotides or polynucleotides, where there is a mismatch between the oligonucleotide or polynucleotide substrate and the template at the ligation junction (Wu and Wallace (1989) Genomics (4):560). Finally, Taq and Pfu polymerases, by virtue of their ability to function at high temperature, are found to display high specificity for the sequences bounded and thus defined by the primers; the high temperature results in thermodynamic conditions that favor primer hybridization with the target sequences and not hybridization with non-target sequences (H. A. Erlich (ed.) (1989) PCR Technology, Stockton Press).

The term “amplifiable nucleic acid” refers to nucleic acids that may be amplified by any amplification method. It is contemplated that “amplifiable nucleic acid” will usually comprise “sample template.” The terms “PCR product,” “PCR fragment,” “amplification product,” and “amplicon” refer to the resultant mixture of compounds after two or more cycles of the PCR steps of denaturation, annealing and extension. These terms encompass the case where there has been amplification of one or more segments of one or more target sequences.

In some forms of PCR assays, quantification of a target in an unknown sample is often required. Such quantification may be determined in reference to the quantity of a control sample. The control sample starting material/template may be co-amplified in the same tube in a multiplex assay or may be amplified in a separate tube. Generally, the control sample contains template at a known concentration. The control sample template may be a plasmid construct comprising only one copy of the amplification region to be used as quantification reference. To calculate the quantity of a target in an unknown sample, various mathematical models are established. Calculations are based on the comparison of the distinct cycle determined by various methods, e.g., crossing points (CP) and cycle threshold values (Ct) at a constant level of fluorescence; or CP acquisition according to established mathematic algorithm.

Some embodiments of the invention may comprise a multiplex assay. As used herein, the term “multiplex” refers to the production of more than one amplicon, PCR product, PCR fragment, amplification product, etc. in a single reaction vessel. In other words, multiplex is to be construed as the amplification of more than one marker-specific sequences within a PCR reaction or assay within the same PCR assay mixture (e.g., more than one amplicon is produced within a single vessel that contains all of the reagents necessary to perform a PCR reaction). In some embodiments, a step prior to performing the PCR (or RT-PCR, quantitative RT-PCR, etc.) reaction can occur such that sets of primers and/or primers and probes are designed, produced, and optimized within a given set of reaction conditions to ensure proper amplicon production during the performance of the PCR;

The algorithm for Ct values in real time-PCR calculates the cycle at which each PCR amplification reaches a significant threshold. The calculated Ct value is proportional to the number of marker copies present in the sample, and the Ct value is a precise quantitative measurement of the copies of the marker found in any sample. In other words; Ct values represent the presence of respective marker that the primer sets are designed to recognize. If the marker is missing in a sample, there should be no amplification in the Real Time-PCR reaction.

Alternatively, the Cp value may be utilized. A Cp value represents the cycle at which the increase of fluorescence is highest and where the logarithmic phase of a PCR begins. The LightCycler® 480 Software calculates the second derivatives of entire amplification curves and determines where this value is at its maximum. By using the second-derivative algorithm, data obtained are more reliable and reproducible, even if fluorescence is relatively low.

The various and non-limiting embodiments of the PCR-based method detecting marker expression level as described herein may comprise one or more probes and/or primers. Generally; the probe or primer contains a sequence complementary to a sequence specific to a region of the nucleic acid of the marker gene. A sequence having less than 60% 70%, 80%, 90%, 95%, 99% or 100% identity to the identified gene sequence may also be used for probe or primer design if it is capable of binding to its complementary sequence of the desired target sequence in marker nucleic add.

Some embodiments of the invention may include a method of comparing a marker in a sample relative to one or more control samples. A control may be any sample with a previously determined level of expression. A control may comprise material within the sample or material from sources other than the sample. Alternatively, the expression of a marker in a sample may be compared to a control that has a level of expression predetermined to signal or not signal a cellular or physiological characteristic. This level of expression may be derived from a single source of material including the sample itself or from a set of sources.

The sample in this method is preferably a biological sample from a subject. The term “sample” or “biological sample” is used in its broadest sense. Depending upon the embodiment of the invention, for example, a sample may comprise a bodily fluid including whole blood, serum, plasma, urine, saliva, cerebral spinal fluid, semen, vaginal fluid, pulmonary fluid, tears, perspiration, mucus and the like; an extract from a cell, chromosome, organelle, or membrane isolated from a cell; a cell; genomic DNA, RNA, or cDNA, in solution or bound to a substrate; a tissue; a tissue print, or any other material isolated in whole or in part from a living subject or organism. Biological samples may also include sections of tissues such as biopsy and autopsy samples, and frozen sections taken for histologic purposes such as blood, plasma, serum, sputum, stool, tears, mucus, hair, skin, and the like. Biological samples also include explants and primary and/or transformed cell cultures derived from patient tissues. In some embodiments, sample may comprise a portion of a non-animal organism, such as a plant (e.g., castor beans or derivatives thereof).

In some embodiments, sample or biological sample may include a bodily tissue, fluid, or any other specimen that may be obtained from a living organism that may comprise additional living organisms. By way of example only, in some embodiments, sample or biological sample may include a specimen from a first organism (e.g., a human) that may further comprise an additional organism (e.g., bacteria, including pathogenic or non-pathogenic/commensal bacteria, viruses, parasites, fungi, including pathogenic or non-pathogenic fungi, etc.). In some embodiments of the invention, the additional organism may be separately cultured after isolation of the sample to provide additional starting materials for downstream analyses. In some embodiments, the sample or biological sample may comprise a direct portion of the additional, non-human organism and the host organism (e.g., a biopsy or sputum sample that contains human cells and bacteria).

With respect to use of the sample or biological sample, embodiments of the claimed methodology provide improvements compared to conventional methodologies. Specifically, conventional methodologies of identifying and characterizing microorganisms include the need for morphological identification and culture growth. As such, conventional methodologies may take an extended period of time to identify the microorganism and may then require further time to identify whether the microorganism possesses and AR markers. Some embodiments of the invention can provide a user with information about any microorganisms present in a sample without the need for additional culturing because of the reliance of nucleic acid amplification and sequencing. In other words, direct extraction of nucleic acids coupled with amplification of the desired markers and downstream sequencing can reduce significantly the time required to obtain diagnostic, AR, and strain identifying information.

The invention may further comprise the step of sequencing the amplicon. Methods of sequencing include but need not be limited to any form of DNA sequencing including Sanger, next-generation sequencing, pyrosequencing, SOLiD sequencing, massively parallel sequencing, pooled, and barcoded DNA sequencing or any other sequencing method now known or yet to be disclosed.

In Sanger Sequencing, a single-stranded DNA template, a primer, a DNA polymerase, nucleotides and a label such as a radioactive label conjugated with the nucleotide base or a fluorescent label conjugated to the primer, and one chain terminator base comprising a dideoxynucleotide (ddATP, ddGTP, ddCTP, or ddTTP, are added to each of four reaction (one reaction for each of the chain terminator bases). The sequence may be determined by electrophoresis of the resulting strands. In dye terminator sequencing, each of the chain termination bases is labeled with a fluorescent label of a different wavelength that allows the sequencing to be performed in a single reaction.

In pyrosequencing, the addition of a base to a single-stranded template to be sequenced by a polymerase results in the release of a pyrophosphate upon nucleotide incorporation. An ATP sulfuryrlase enzyme converts pyrophosphate into ATP that in turn catalyzes the conversion of luciferin to oxyluciferin which results in the generation of visible light that is then detected by a camera or other sensor capable of capturing visible light.

In SOLiD sequencing, the molecule to be sequenced is fragmented and used to prepare a population of clonal magnetic beads (in which each bead is conjugated to a plurality of copies of a single fragment) with an adaptor sequence and alternatively a barcode sequence. The beads are bound to a glass surface. Sequencing is then performed through 2-base encoding.

In massively parallel sequencing, randomly fragmented targeted nucleic acids and/or amplicons are attached to a surface. The fragments/amplicons are extended and bridge amplified to create a flow cell with clusters, each with a plurality of copies of a single fragment sequence. The templates are sequenced by synthesizing the fragments in parallel. Bases are indicated by the release of a fluorescent dye correlating to the addition of the particular base to the fragment.

Nucleic acid sequences may be identified by the IUAPC letter code which is as follows: A—Adenine base; C—Cytosine base; G—guanine base; T or U—thymine or uracil base, M—A or C; R—A or G; W—A or T; S—C or G; Y—C or T; K—G or T; V—A or C or G; H—A or C or T; D—A or G or T; B—C or G or T; N or X—A or C or G or T. Note that T or U may be used interchangeably depending on whether the nucleic acid is DNA or RNA, A sequence having less than 60%, 70%, 80%, 90%, 95%, 99% or 100% identity to the identifying sequence may still be encompassed by the invention if it is able of binding to its complimentary sequence and/or facilitating nucleic acid amplification of a desired target sequence. In some embodiments, as previously mentioned, the method may include the use of massively parallel sequencing, as detailed in U.S. Pat. Nos. 8,431,348 and 7,754,429, which are hereby incorporated by reference in their entirety.

Some embodiments of the invention comprise multiple steps and/or processes that are carried out to execute the universal tail indexing strategy to prepare amplicons corresponding to desired markers for sequencing. In some embodiments, one or more makers for a given sample or template can be selected, as described above. Some embodiments of the invention can be used in conjunction with an analysis of one or more markers (e.g., genes/alleles) associated with a particular phenotype (e.g., resistance to one or more pharmaceuticals, such as antibiotics). By way of example only, some embodiments of the invention can be used to detect and/or quantify the development of antibiotic resistance in populations of patients infected with an organism. As such, in some aspects, prior to performing additional steps, an investigator can assess the markers present within the genome of the organism to determine which markers are implicated in the development of antibiotic resistance. For example, markers can be selected that may contain a SNP or other change or alteration that can confer at least partial antibiotic resistance. In other aspects of the invention, markers can be selected that are not implicated in antibiotic resistance, but are associated with other phenotypes/genotypes that are desirable for further analysis.

After selection of the markers, marker-specific primers/oligonucleotides can be designed for the amplification of the markers to produce the desired amplicons, as detailed above. As is known in the art, a forward and a reverse marker-specific primer can be designed to amplify the marker from a nucleic acid sample. In some embodiments, the forward and reverse primers can be designed to produce an amplicon (e.g., some or all of the sequence of the marker) of a desired length. For example, the length of the amplicon may comprise approximately 50 base pairs (bp), 100 bp, 150 bp, 200 bp, 250 bp, 300 bp, 350 bp, 400 bp, 450 bp, 500 bp, 1,000 bp, or any size amplicon greater in size or therebetween.

As previously mentioned, some embodiments of the invention may include a multiplex PCR reaction. For example, marker-specific primers can be designed for multiple markers or multiple regions of the same marker such that multiple amplicons of between about 50 bp and 1,000 bp are being produced within a single PCR reaction vessel. In other words, the forward and reverse primers can be designed to function within a given set of temperature parameters such that more than one amplicon can be successfully amplified from a given template within a single PCR reaction mixture. As such, multiple amplicons can be prepared using the universal tail indexing strategy for sequencing preparation.

In some embodiments, the forward and reverse primers that have been designed for each of the markers can be modified to include a universal tail. For example, the universal tail sequences can be relatively or completely unique sequences of nucleotides that are coupled to the 5′ ends of some or all of the forward and reverse marker-specific primers. In some aspects, the universal tail sequences can be selected such that there is little to no overlap in sequence between portions of the markers that are being amplified and the universal tail sequences. Moreover, the universal tail sequences can comprise a length between ten and twenty nucleotides in length. In some embodiments, the universal tail sequences can be any other length, as desired by the user to meet the needs and requirements of the reaction. As such, the universal tail sequences can exhibit a relatively negligible impact on binding of the forward and reverse marker-specific primers to the template sequence to enable amplification. Moreover, as a result of being included on the 5′ end of the forward and reverse marker-specific primers, the universal tail sequences will form a portion of the resulting amplicons. In addition, in some aspects of the invention, the sequences selected for the universal tail sequences can be at least partially correlated with the chemical composition of the template nucleic acids. For example, in some aspects, the sequences selected for the universal tail sequences can be at least partially correlated with the G-C content of the organism from which the template is isolated.

In some aspects, some or all of the universal tail sequences can be at least partially unique. In some embodiments, each of the 5′ ends of all of the forward marker-specific primers within a given PCR assay mixture can comprise the same or a similar universal tail sequence (e.g., a first universal tail sequence or UT1). Similarly, each of the 5′ ends of all of the reverse marker-specific primers within the same PCR assay mixture can comprise a second universal tail sequence (UT2) that differs from the first universal tail sequence. As such, each respective sample from which a template sequence is used in the multiplex PCR assay will have two unique universal tail sequences. Accordingly, each forward and reverse marker-specific primer within a multiplex PCR mixture will include a unique universal tail sequence. For example, if the PCR includes 35 different samples, 35 universal tail sequences can be employed for the forward primers in each of the 35 unique reactions (i.e., not including technical replicates) and 35 universal tail sequences can be employed for the reverse primers in each of the 35 unique reactions (i.e., not including technical replicates). Overall, the forward and reverse marker-specific primers that each comprise the universal tail sequences can comprise a generally short length (e.g., 25-50 bp), which can facilitate simultaneous amplification of multiple targets in a single reaction.

In addition, some embodiments of the invention may comprise performing quantitative PCR to optimize the multiplex PCR assay. For example, after design of the forward and reverse marker-specific primers that each include a universal tail sequence, the contemplated multiplex PCR assays can be performed using quantitative PCR (e.g., using DNA as a template) to assess relative quantities of the amplicons produced. Accordingly, the sequence coverage of each amplicon is considered to be equal if the quantities of the amplicons produced by the multiplex quantitative PCR appear to be equal. If the quantities of the amplicons produced by the multiplex quantitative PCR do not appear to be equal, the forward and/or reverse marker-specific primers can be altered and re-optimized until adequate quantities of amplicons are produced.

After design and adequate optimization of the multiplex PCR assay comprising multiple forward and reverse marker-specific primers that each include universal tail sequences, the multiplex PCR can be performed to obtain the amplicons associated with the above-described markers. In some embodiments, template that has been previously isolated from a sample can be used for the amplification of the amplicons. In some aspects, multiple PCR reaction replicates can be performed for each sample template and one or more control templates.

In some embodiments, after successful production of the amplicons during the multiplex PCR assay, the resulting amplicons can be further processed to provide sequencing-ready amplicons. For example, some embodiments of the invention may comprise an indexing extension step. In some aspects, the indexing extension step may comprise extending the optimized multiplex amplicons using a set of indexing and common primers that recognize the respective universal tail sequences used for the particular group of amplicons in a minimal cycle PCR assay (e.g., 5-10 total cycles). In particular, each multiplex set of amplicons to be sequenced can be extended with a different set of index oligonucleotides and common oligonucleotides that recognize UT1 and UT2, respectively. In some aspects, the index sequence of the index oligonucleotides can be custom designed to allow for the selection of an index sequence from potentially thousands of different index sequences.

After this step, the resulting products include a set of amplicons for each sample/template that comprise the same index and any necessary sequences that may be required for a particular sequencing platform (e.g., platform sequences associated with the ILLUMINA® Next Generation sequencing platform). Thereafter, the resulting extension-reaction products can be quantified, pooled, and sequenced using a desired platform. In some aspects, the inclusion of the universal tail sequences on the index and common primers can coincide with the use of genomic and index read primers in the mixture of sequencing primer reagents. For example, some embodiments of the invention are capable of pooling multiple amplicons with multiple indices in a single sequencing run to provide 40,000×-95,000× coverage across the amplicons. In other embodiments, the systems and methods associated with the invention can be configured to provide any level of sequencing coverage that is desirable to the user (e.g., higher or lower that the coverage levels discussed above). In some embodiments, after sequencing and generation of the sequence data, the resulting data can be demultiplexed and the sequence files can be aligned to the appropriate references sequences for subsequent sequence analyses.

Embodiments of the invention offer additional advantages relative to conventional systems. For example, some embodiments of the invention comprise the use of PCR before sequencing such that only limited amounts of starting material are necessary and the starting material need not be of high quality (e.g., genomic DNA, crude DNA extracts, single stranded DNA, RNA, cDNA, etc.). In contrast, many conventional sample preparation systems may require relatively large amounts of starting material of relatively high quality, which can limit the use of these systems. Moreover, the inclusion of non-desirable template materials can also interfere in one or more downstream processes in conventional systems and methods. For example, if an investigation is being conducted that focuses on one or more organisms that may be associated with another organism (e.g., bacteria associated with a human); the sampling of the target organism may result in template contamination from the host organism.

In particular, in some aspects, obtaining samples of pathogenic or commensal bacteria from, on, or within a human may also result in the collection of human tissue. As such, when isolating the template, human nucleic acids may contaminate the bacterial template. Some embodiments of the invention are configured such that the contaminating template (e.g., from a human) would not interfere with downstream processes, including sequencing. For example, some embodiments of the invention operate such that only a limited amount of starting template (e.g., 500 femtograms or greater) can be used. Moreover, some embodiments are also configured such that the starting material (e.g., template contaminated with foreign nucleic acids) can still produce the required amplicons for sequencing in the presence of more than a 1,000-fold excess of contaminating template with no discernible inhibition of the multiplex PCR.

In certain aspects, the present invention provides an assay that works with as little as about 1 pg, about 900 fg, about 800 fg, about 700 fg, about 600 fg, about 500 fg, about 400 fg, about 300 fg, about 200 fg, or about 100 fg of genomic DNA.

Examples

The inventors employed embodiments of the methods detailed herein to assess the presence of microorganisms in control samples from respiratory, wound, nasal swab, and urine specimens using oligonucleotides/primers detailed in Tables 1 and 2 to amplify desired markers. Thereafter, the resulting amplicons were sequenced using next-generation sequencing technology to obtain information on the identity and AR characteristics of the microorganisms in the samples.

As illustrated in Table 4, the inventive methodology produced extremely reliable results, compared to standard/conventional culture methods. Moreover, as illustrated by the samples that include the *** indication, the claimed methodology was also able to reveal the presence of an AR marker, which was not detected using the traditional culture methodology. Moreover, as illustrated in Table 5, by detecting organisms that were not previously detected using traditional culture-based methods, the method further shows increased sensitivity compared to the culture-dependent methodology.

As illustrated in Tables 6, 7, and 8, the inventive methodology was used to identify microorganisms from different sample types. For example, in Table 6, the inventive methodology was used to identify the listed species and the listed antibiotic resistances in 27 respiratory specimen samples from subjects with cystic fibrosis. Similarly, in Table 7, the inventive methodology was used to identify the listed species and the listed antibiotic resistances in 24 respiratory specimen samples from subjects with chronic rhinosinusitis. Finally, in Table 8, the inventive methodology was used to identify the listed species and the listed antibiotic resistances in 38 respiratory specimen samples from subjects with various respiratory diseases.

It should be understood from the foregoing that, while particular embodiments have been illustrated and described, various modifications can be made thereto without departing from the spirit and scope of the invention as will be apparent to those skilled in the art. Such changes and modifications are within the scope and teachings of this invention as defined in the claims appended hereto.

TABLE 1 Oligonucleotides/Primers for Use in Identifying Bacterial Species Target SEQ ID purpose Target ID Assay Sequence NO: Species ID Klebsiella  Kp_M1_UT1v  CGTTTCACAACTGCGGATG   1 pneumoniae (Cluster 1245) TGGCGGTCATGTTCTTACTC   2 Kp_M1_UT2v  TTCACACCGCCATCGTC   3 (Cluster 1245) CAGCATCTCCACCGACAG   4 Kp_M1_UT1nv  CGTTCCTCACCGTAGTGG   5 (Cluster 4240) TCCAGCGTGACATAATCGG   6 Kp_M1_UT2nv  TTTCCACCTACGCCGATAAAG   7 (Cluster 4240) CCAGCGGAATAACCAGGAC   8 Kp_M2_UT1v  GGCGGCGATGAGTTTGT   9 (Cluster 1825) ATGTTGCGGATAGCCTGATAG  10 Kp_M2_UT2v  CGCTCCACTATCAGGCTATC  11 (Cluster 1825) TTCGGCGATGGGAATAAACA  12 Kp_M2_UT1nv  TGCCTATCGCCACTTTATTGA  13 (Cluster 2858) CGGTCGTTAATCGCCTTCT  14 Kp_M2_UT2nv  CCTCAGGTACGCTCATTCG  15 (Cluster 2858) TCGTCACATCCCTCCTCTT  16 Species ID Serratia  Smar_UT1 GATCAGCAGCAAACGGTGAC  17 marcescens GGCGATGTAATCCTGCGAGA  18 Species ID Proteus  Pmbs_UT1 GGGATATCCGTGGAATGCGT  19 mirabilis TAATGTGATCACCGCTCCCG  20 Species ID Providencia  Pal_UT1 ACGAGCCAGCCTGATGAAAA  21 alcalifaciens CATCGCAACTGCTGCATCTC  22 Species ID Providencia  Pst_UT1 GCCTTGCGCCTTAGTTTGTT  23 stuartii GGCTATCCATTTTCCAGCCG  24 Species ID Enterococcus  Efs_UT1 TTCTTTTCCAGGAGCAACGC  25 faecalis AGCAAGACAGAAATAAGTAAAAAGA  26 Efs_UT2 TCTTCGTCATGGTGSGTTTC  27 AACGGAACATGGTGAGCAAC  28 Species ID Enterococcus  Efm_UT1 GKTTTGATGGCTGGGTCAGT  29 faecium TGTTTGGCTTTTTGCAGTTG  30 TACTTRGCTTTTTGCAGTTG  31 Efm_UT2 TCAGTGAAAACRACCCACGA  32 ATYGCTGCTGTCCGAGTTCT  33 Species ID Klebsiella  Koxy_UT2 CCGTCGCCGTATTACTGAT  34 oxytoca TCTCTACAACACGCTACCCTA  35 Species ID Klebsiella  Koxy_UT3 GGTGAGAACGATGTGATTGTG  36 oxytoca TGACCCAAAGGCGATTCG  37 Species ID Pseudomonas PSAR_28621 GAAGCGGTTGAGGAACAG  38 aeruginosa ACCCACGACATGATGTAC  39 PSAR_27569 GGACGATCCATTCCATACCG  40 GACGAAGCGGTGATCCAC  41 Species ID Staphylococcus  Sa_M1_UT1 ATAGGTGTGGCTTTTGTAGGG  42 aureus CTGCTGCTAATAACGCTTGC  43 Sa_M2_UT1 ATGGTTATGAAATTGTTGGTGATGAA  44 CCGTTGCTTGATATTCTTTCGTAT  45 Sa_M4_UT1 TACGAAATCAGAAGTGGCTCAA  46 ACGTTAAATCCTGCATTTTCCAA  47 Sa_M4_UT2 TAGCGTTGGTATTAAGTGGTTGT  48 GTCATAGCATAGTTCGGGTCA  49 Genus and Staphylococcus tuf_UT1 ACWGGCCGTGTTGAACGTG  50 species ID CACCAGCTTCAGCGTAGTCTAAT  51 tuf_UT2 CTCAACWGGCATCATGAATGGTTT  52 AGGTGACGATGTRCCTGTAATC  53 Species ID Escherichia  Ec_M1_UT CGTTGTTTGCGACCYGTATA  54 coli AATGTAAATTCGCTGRGATCGT  55 Ec_M2_UT CGCCTGGCTCTGTTTCA  56 AGCAAGTGCATTACGAGTCT  57 Species ID Acinetobacter  AB_marker1 GTCTGTTGAATGATGATGTATGTCG  58 baumannii ATCCCATTTTACAAATGGCAAAACA  59 TGCAGAACTAGCCCATTTTACA  60 TGCWGAACTAKCCCATTTTACA  61 Species ID Acinetobacter  Ab_M2_UT1 TTTAGCGRACAGATTTGGTTTACA  62 baumannii CGGTTGCCTTGCTGAGTT  63 Ab_M2_UT2 TCCGYAAACCTCAACTCATTT  64 GCCAGTGAACCATCTAATACAGT  65 Ab_M3_UT1 TAGAGCAGCAACAAATCAACAAGA  66 TTATTATGAGTCGCCTTGGCAATT  67 Ab_M3_UT2 TAGAGCAGCAACAAATCAACAAGA  68 TCGCATGGCTTCTGACTCA  69 Acinetobacter Acb_M2_UT1 AAATTGCYAAAGCACAAGGTTT  70 calcoaceticus- CGGGAATTGCYTCATGGTAAG  71 baumannii complex Acb_M3_UT1 GATAGCGATTACTCGGTTCCATC  72 CCTGTGCCTAAAACCAGTGAAA  73 Species ID Streptococcus Sp_M1_UT2 TCCTGATATAATCGGTGTCACAAG  74 pneumoniae AGAACAAGAGGTATGTCATCTAACTT  75 Sp_M2_UT1 CTGATGGATATGGAGACATTAAGGAT  76 GTCCAATTATATGCGGATCTATACCT  77 Sp_M2_UT2 CTGATGGATATGGAGACATTAAGGAT  78 AATTAGTTGAGTAGCCATGACAGT  79 Sp_M3_UT1 TACGGTGTAAGTGCTGATAAAGG  80 GCTTCAAAGTTAAGTCCATCCAAAT  81 Species ID Streptococcus  GBS_UT1 GCCAACCGTGGTATGTCA  82 agalactiae TTCTGCCGGGTTTCTTTG  83 GBS_UT2 CTCGTGCTGCTACTTCTC  84 CGTGGATGTGCTYGTTAACAAC  85 Species ID Enterobacter Encl_M1_UT AACTTRTCCTTGTGCTTGC  86 cloacae group ACATAGTCGTTGGCATACAGA  87 ATTGTTGATGACTGTTCCTCTTC  88 CGACGAYGATGACGAATG  89 CGCAATTAAGTCGGTCCTG  90 Species ID Enterobacter Encl_M2_UT CCTTCAACGTGRATGTTCAG  91 cloacae group AATWCCYACTTCGCCTTCA  92 TGGCGTTCTGGAYGTCAA  93 AGTTGTTTATACCGCCAAAGC  94 AGTTGTCTACACTGCCAAAGC  95 Species ID Enterobacter  Eaer_M1_UT ACCCAAAAGTATTCTGATTGTTGAG  96 aerogenes ATGAGGTCTTATTATCGGTCAACTG  97 Species ID Enterobacter  Eaer_M2_UT AATCGGCAATACCAGCAGTT  98 aerogenes CCTTCACGGAATAACATATCCAGAT  99 Species ID Streptococcus  Spyo_UT1 GCTTATTGCTAATGACTGTGCTTAT 100 pyogenes TGCCGACATTGACAACCATA 101 Species ID Streptococcus Sdys_UT1 CATCTGCTTGACCTTTATGAAAC 102 dysgalactiae GTGAGGCTAACACATCAAACTAG 103 Species ID Streptococcus Sdys_UT2 ATGCGGGAGGTCTGTTTCTAC 104 dysgalactiae CCAGCCGGTAAAGAAACTC 105 Species ID Streptococcus  Sequi_UT1 GTCAAGCACCTTAYCACCATCTAG 106 equi GGCATGCTTGTGAACAACA 107 Species ID Streptococcus  Sequi_UT2 GTGCCRATTGAGGATCTGGTTTC 108 equi CYGTTGGACCACTTCCTGTCAT 109

TABLE 2 Oligonucleotides/Primers for Use in Identifying Antibiotic Resistance in Bacteria SEQ ID Target purpose Target ID Assay Sequence NO: B-lectam blaKPC KPC_UT1 CGTCTAGTTCTGCTGTCTTGT 110 resistance ACCGTCATGCCTGTTGTC 111 KPC_UT2 TTGTTGATTGGCTAAAGGGAAAC 112 CAGACGACGGCATAGTCATT 113 B-lectam blaNDM NDM_UT1 GGACAAGATGGGCGGTATG 114 resistance CGGCGTAGTGCTCAGTG 115 NDM_UT2 CAACTGGATCAAGCAGGAGAT 116 CGACAACGCATTGGCATAAG 117 Aminoglycoside rmtA rmtA_UT1 GAATTGGACTGCCTCTACGATT 118 resistance GCACGCCCATACAGATGT 119 Aminoglycoside rmtB rmtB_UT1 AAGGCATGGAGGCGAAC 120 resistance AAGTATATAAGTTCTGTTCCGATGGT 121 Aminoglycoside rmtC rmtC_UT1 AATACTCCACACTTTATCCACCAA 122 resistance TTCTTGCGAACCTCCTTCTC 123 Aminoglycoside rmtD1 and rmtD2 rmtD1_&_D2 AACGATGCGACGATCCATT 124 resistance GCGATTTGCTGTGCGAAA 125 Aminoglycoside npmA npmA CCGCTTGCTGGTACATATCTA 126 resistance CCTATCTCGTCCGCTATCTG 127 Aminoglycoside armA armA ACTATTCTGCCTATCCTAATTGGG 128 resistance TCATTTAATGTTGCGACTCTTTCA 129 fluoroquinolone gyrA gyrA_ACBA_UT1 ATGACTATAACAAAGCYTACAAGAAATC 130 resistance ACAATGGTTTCATAAACAGCTAAGTC 131 gyrA_PSAR_UT1 AACAAGCCCTACAAGAAATCC 132 CGCACTTCGGTGTATCG 133 gyrA_PSAR_UT2 AACAAGCCCTACAAGAAATCC 134 CTCGGTGCCATCGTAGT 135 gyrA_staph_UT1 CATTGCCAGATGTTCGTGAC 136 GCCATCAACAAGCGGATAAC 137 gyrA_Ecoli_UT1 AAATCTGCCCGTGTCGTT 138 ACCATCCACCAGCATGTAAC 139 gyrA_Ecoli_UT2 CTCCTATCTGGATTATGCGATGT 140 CGTCAATAGAACCGAAGTTACC 141 gyrA_Kleb_UT1 CAATGACTGGAACAAAGCCT 142 CGATGGAACCAAAGTTACCC 143 fluoroquinolone parC parC_PSAR_UT1 TTGTAGTGTTCCAGGTCGTC 144 resistance CCGTCTGCTATTGTTCAAGG 145 parC_Kleb_UT1 GAAATTCAAAAAGTCCGCCC 146 GGATAGCGGTAAGAGAACGG 147 parC_Kleb_UT2 CAGCGCGAAATTCAAAAAGT 148 GCGAAAGATTTGGGATCGTC 149 parC_Ecoli_UT1 GTTCTCTTACCGTTATCCGC 150 TATTTCGACAACCGGGATTC 151 parC_Ecoli_UT2 TGTGTATGCGATGTCTGAAC 152 ATATTTCGACAACCGGGATTC 153 parC_ACBA_UT1 GAGCGAGCTAGGCTTAAAAA 154 TCCCCTGACCTTCGATTAAA 155 parC_ACBA_UT2 GTACGTCATTATGGACCGTG 156 CTATAAGCCGAGAGTTTGGC 157 parC_staph_UT1 TCCGTAAAAGTGCGAAAACA 158 AGCTTCAGTGTAACGCATTG 159 parC_staph_UT2 CCAGATGTTCGTGATGGTTT 160 CTTAGCTTCAGTGTAACGCA 161 Fluoroquinolone QnrA qnrA_UT1 TAGAGTTCAGGGAGTGCGAT 162 resistance CCGAGCAGAAGTACATCTTATGG 163 qnrA_UT2 GATTTGAGYGACAGCCGTTT 164 GCAGAAGTACATCTTATGGCTGA 165 Fluoroquinolone QnrC qnrC_UT1 GCTAATTTCTCACAGGCAAACTTT 166 resistance ACAACCCGTAATGTAAGCAGAG 167 QnrD qnrD_UT1 GTTTGATTGGTCTTTGGCTGATT 168 CCATCCAACTTCACTCCATCT 169 qnrD_UT2 CGACAGGAATAGCTTGGAAGG 170 CCAGTTATCACAGTGCCATTC 171 QnrS qnrS_UT1 CAATTTATGCCACGCCGAAC 172 TAATTTATGTCACGCCGAAC 173 GATAAACAACAATACCCAGTGCTT 174 qnrS_UT2 GTGCTAACTTGCGTGATACGA 175 TCCATATTGGCATAGGAAAGATTACA 176 TCCATATTGGCATAAGACAGGTTACA 177 QnrB qnrB-C1_UT1 GACGTTCAGTGGTTCRGATCT 178 KGCTCGCCAGTCGAAAGT 179 qnrB-C1_UT2 CGACGTTCAGTGGTTCRGATCT 180 GCKGCTCGCCAGTCGAAA 181 qnrB-C2_UT1 ACCAATCTAAGCTACGCCAACTT 182 CCTGAGTTCCCATCCAGCG 183 qnrB-C3_UT1 TACGCACTGTGATTTGACCAAT 184 GGAKCAACGATGCCTGGTAG 185 qnrB-C3_UT2 CGCATATATCACCAATACCAACTT 186 GTTCCAGGAKCAACGATGCC 187 B-lactamase blaCTX-M genes CTX-M-G1_64_UT1 CCGTCACGCTGTTGTTAGG 188 production CGCTCATCAGCACGATAAAGT 189 CTX-M-G1_64_UT2 CGCTGATTCTGGTCATTTACTTC 190 ACGGCTTTCTGCCTTAGGT 191 CTX-M-G1_UT1 CGATGTGCAGCACCAGTAA 192 TCGGTTCGCTTTCACTTTTCT 193 CTX-M-G1_UT2 GACGATGTCACTGGCTGAG 194 CCACAACCCAGGAAGCAG 195 CTX-M-G2_74-75_UT1 TGGCGCAGACCCTGAAAA 196 ATATCGTTGGTGGTGCCATAA 197 CTX-M-G2_74-75_UT2 ATGGCGCAGACCCTGAAA 198 CCGCTGCCGGTTTTATCG 199 CTX-M-G8_G25_UT1 GAGCCGACGCTCAACACC 200 CCCGACAACCCACGATGT 201 CTX-M-G8_G25_UT2 GCTCAACACCGCGATCCC 202 CCCGACAACCCACGATGT 203 CTX-M-G9_UT1 TTCGTCTGGATCGCACTGA 204 GATGATTCTCGCCGCTGAAG 205 CTX-M-G9_UT2 CGCTGGTTCTGGTGACCTA 206 GATGATTCTCGCCGCTGAAG 207 Dihydrofolate dfrA genes dfrA1_UT1 AATGGCTGTTGGTTGGACG 208 reductase CATACTTTCGGTTGGGTAATGCT 209 production (DNA dfrA15_UT1 AATATGCCGTTGTAACTCGTTCA 210 synthesis) ACACAATCACATGATCCGTTATCG 211 uninhibited by dfrA16_UT1 AGTATGCAGTTGTAACTCGCTCTA 212 trimethoprim CACCACCACCAGAAACGATAAC 213 dfrA14-30_UT2 GTGATTGGTTGCGGTCCA 214 CCCGCCACCAGACACTAT 215 dfrA6-31_UT1 YGAGAATGGAGTAATTGGCTCT 216 WATTTCACCACCACCAGAAACAAA 217 dfrA26-13_UT1 GGGWGCCAATCGGGTTAT 218 CTCAGTGAGTCTGCGAAA 219 CTCGGTGAGCCTGCGAAA 220 dfrA8_UT1 AAAGACTACGAGCAGAATGGC 221 ACGGTAAGTGAAGTAAGTGTGAAG 222 dfrA3b_UT1 AACGCTGCCATTGTTACCA 223 AAGCCTTGAAGTGTTCTGGAG 224 dfrA9_UT1 AAGACAGGAGGTATCGGATTTGA 225 CGTAGGCAGCTAAGTTCTCGTA 226 dfrA24_UT1 AAGACCGCATCAATATCGTCATC 227 CATAGCAAGCCGTCCAAGAA 228 dfrA27-28_UT1 AAGACTCTTACGAACCATGTTGTT 229 CCTCTGGCTCGGAATCTATTG 230 dfrA25_UT1 AAGCACTGACCTATAACCAATGG 231 CCCAGGAATGTTCGGAAAGAAA 232 dfrA10_UT1 AAGCATTCAGAGACACAACCAA 233 AACCAACACCACCAATGACAT 234 dfrA32_UT1 AAGGTGAGCAGCTAATCTTTAAGG 235 TGACCCTGAAATTCCATTCTTTGA 236 dfrA20_UT1 AAGTCGCACAACATCTTGAAGG 237 AGATTTGAGCACCACCAATAATGA 238 dfrA23_UT1 AATCAATATCACGACAGCGATCAA 239 CTTCACGGGATGGGTCTCA 240 dfrA7_UT1 AATCAGTGGCTCCTTGTTGG 241 GGAAGAACACCCATAGAGTCAAAT 242 dfrA29_UT1 AATCAGTGGCTTCTTGTCGG 243 GTGGATGATAGATAAGTGGATGGT 244 dfrA17_UT1 AATGGCGTAATCGGTAGTGG 245 GCTTGAAATTCCGTTCTTTGACA 246 dfrA18_UT1 ACGCATTGCTGTCATTGGT 247 CTCGCTGGCACTGGAATC 248 dfrA3_UT1 ACTCTATGCCGAGGCTCTG 249 CGCTGACGACTCAAGGTAAC 250 Dihydrofolate dfrB genes dfrB1-8_UT1 WATGGGAGATCGCGTGCG 251 reductase GCWGTACCACCCGACAATCT 252 production (DNA dfrB2-7_UT1 GCAGGGTCAAGTYGTCGG 253 synthesis) TCGGACTCGACSGCATAG 254 uninhibited by dfrB3_1_UT1 ACCCGACAACTTGACCCT 255 trimethoprim ACCAACACAACAATGGAGTCA 256 dfrB4_UT1 AATCTCACCCAGGCTCAGT 257 CCGTTCAAGCGCAGTCAT 258 dihydropteroate sul genes sul1_UT1 GCTGGTGGTTATGCACTCAG 259 synthase (DNA CGCCCAAGAAGGATTTCCG 260 synthesis) sul1_UT2 CGTGCTGTCGAACCTTCAA 261 uninhibited by GCTGGACCCAGATCCTTTACA 262 sulfonamides sul2_UT1 CATCATTTTCGGCATCGTCAAC 263 GCGACAAGGCATAGGCTT 264 sul2_UT2 GTCAACATAACCTCGGACAGTT 265 CTCGGCCATCAGCTTACG 266 sul3_UT1 AAAGCCTTAATGACAGGTTTGAGT 267 GAAGATGGAGCAGATGTGATTGAT 268 sul3_UT2 GGCAAAGTCAGATTGCAAACTTG 269 CCTCTTCCGGATTCGTTTCAAC 270 Vancomycin- Staphylococcus rpoB VISA_rpoB-481_UT1 CCAGGTCCTAATGCTGATAGACG 271 intermediate S. (VISA) ACCGTCGTTTACGTTCTGTAGGTG 272 aureus (VISA) VISA_rpoB-481_UT2 CCAGGTCCTAATGCTGATAGACG 273 GGACCAAGCAAAYCCATTAGCT 274 Staphylococcus linA linA_UT1 GTGAAGGCATCCAATSAACTT 275 antibiotic AAACMACAAAGAGAACACAGAGAT 276 resistance mecA mecA_UT1 GGAACGATGCCTATCTCATATGCT 277 ATAGCGTCATTATTCCAGGAATGCA 278 vanA vanA_UT1 CGGCTCGACTTCCTGATGA 279 TGTGCGGTATTGGGAAACAG 280 aacA aacA_UT1 GCCACACTATCATAACCACTACCGA 281 TCCAAGAGCAATAAGGGCATACCAA 282 blaZ blaZ_UT1 ACACTCTTGGCGGTTTCACT 283 CCTAAGGGCCAATCTGAACCTATT 284 ermA ermA_UT1 CAACCATTGATTTCAAAGAAGGACTAC 285 TCAAAGCCTGTCGGAATTGGT 286 ermC ermC_UT1 ATTTAATCGTGGAATACGAGTTTGCTAA 287 CGTCAATTCCTGCATGTTTTAAGG 288 tetK tetK_UT1 AGTTTGAGCTGTCTTGGTTCATTG 289 TGCAGCAGATCCTACTCCTTGTAC 290 tetM tetM_UT1 CTTTCTGGGCTTCCATTGGTTTATC 291 CGAGCTCTCATACTGCATTCCA 292 msrA msrA_UT1 CTTCTTCCAAATGTTCCATTCTTTTT 293 ACCAGATCGTTTAAGTGCATCAAA 294 cfr cfr_UT1 AACGAAGGGCAGGTAGAAGC 295 TGACCACAAGCAGCGTCAAT 296 cfr_UT2 GTGAGGAACGCAGCAAATTGA 297 GCTTCTACCTGCCCTTCGTT 298

TABLE 3 Oligonucleotides/Primers for Use in Genetic Characterization of Bacteria Target SEQ purpose Target ID Assay Sequence ID NO: MRSA ID- MRSA-orfX MRSA-orfX_UT1 GGATCAAACGGCCTGCACA 299 orfX junction MRSE ID- MRSE-orfX MRSE-orfX_UT1 TGGCTCCAATGGTYTACACCAA 300 orfX junction GTCAAAAATCATGAACCTCATTACTTATG 301 ATTTCATATATGTAATTCCTCCACATCTC 302 CAAATATTATCTCGTAATTTACCTTGTTC 303 CTCTGCTTTATATTATAAAATTACGGCTG 304 CACTTTTTATTCTTCAAAGATTTGAGC 305 SCCmec typing S. aureus ccrB2 SCCmec_ccrB2_UT CTCATGTTACARATACTTGCG 306 CCTTGATAATAGCCTTCTTGG 307 S. aureus mecl SCCmec_mecl_UT CGTTATAAGTGTACGAATGGTTTTTG 308 TCATCTGCAGAATGGGAAGTT 309 S. aureus IS1272J SCCmec_IS1272J_UT GAAGCTTTGGGCGATAAAGA 310 GCACTGTCTCGTTTAGACCAATC 311 S. aureus ccrC SCCmec_ccrC_UT TCCAGTCTATAAAGGSTATGTCAG 312 ACTTATAATGGCTTCATGCTTACC 313 S. aureus ccrB1 SCCmec_ccrB1_UT ACCACAAACACACTTAAAGATG 314 CAATTTCAAGTATTTGGTCCATAAC 315 S. aureus ccrB3 SCCmec_ccrB3_UT AACACAACGAACACATTGAAAG 316 CGTATTTCTCAATCACATCAGC 317 S. aureus ccrB4 SCCmec_ccrB4_UT CGAAGTATAGACACTGGAGCGATA 318 GCGACTCTCTTGGCGTTTA 319 S. aureus mecC2 SCCmec_mecC2_UT TCAGTTCATTGCTCACGATATG 320 GCCAACGGCTACAGTGATAA 321 SCCmeclVa-J1 SCCmeclVa-J1_UT CAGGATATTTTTCAAACTCCTTCA 322 TGGAGGACCAAGGATATTCG 323 SCCmeclVa SCCmeclVa_UT CCTTTGAATGCCCTCCATGAATAAAAT 324 GCATATAGAAAAGATAGAAGTTCGAAAGA 325 S. aureus MRSA sea sea_UT TATGGCTAGACGGTAAACAAAATACAG 326 virulence CTCTGAACCTTCCCATCAAAAACATC 327 MRSA seb seb_UT TTACTGTTMGGGTATTTGAAGATGG 328 CCGTTTCATAAGGYGAGTTGT 329 E. coli Shiga toxin genes stx1_UT ATGTCAGAGGGATAGATCCA 330 virulence TATAGCTACTGTCACCAGACAAT 331 stx2_UT AGTTCTGCGTTTTGTCACTGTC 332 CGGAAGCACATTGCTGATT 333 E. coli aggR EAEC_aggR_UT GATACATTAAGACGCCTAAAGGATGC 334 CCTTTTGACCAATTCGGACAACT 335 T3SS in E. coli escV_UT TGGAATAATCATCATCATTACAGCCA 336 GAGTCATATCACGATCTTATTCTGGC 337 E. coli virulence bfpA_UT TACCAGTCTGCGTCTGATTCC 338 ACGTTGCGCTCATTACTTCTG 339 E. coli (and Shigella) EIEC_IpaH3_UT TGAGTTACCTGAATCACTGGAAG 340 invasion antigen TCGAGGATGATAGTGCAGGTC 341 E. coli enterotoxins ETEC_eltA_UT CTGCGTTAGGTGGAATACCAT 342 CTGGGTCTCCTCATTACAAGTATC 343 ETEC_estA_UT GTTCCAGCCTGCCATCTG 344 TCGCCAGCAACACTTCAG 345 E. coli UPEC UPEC_fyuA_UT AAGCACGCTGGTGGTTAC 346 CTGGATGGTGTTGGTGGAA 347 Klebsiella wzi gene of cps locus wzi_UT CGCGAGYGCTTTCTATCTTG 348 capsule type GAGASCCACTGGTTCCAGAA 349 CONTROL PCR IPSC IPSC_UT1 ACCCAACTGAATGGAGCGGGCGGA 350 CGAAAACCCTTGAGCACAG ACGCACTTGACTTGTCTTCGCCGGG 351 ATGCCTTACCTAGACGCAATGA IPSC_UT2 ACCCAACTGAATGGAGCGCGGCAGC 352 CGTTGAGGCAAAAGTGATAC ACGCACTTGACTTGTCTTCCGAGTTC 353 CGTCCGGTTAAGCGTGACAGTC

TABLE 4 Organisms Detected Correctly Compared to Culture Methods Organisms Detected Correctly Compared to Culture Methods/Total Tested Specimen Type K. pneumoniae S. aureus S. pneumoniae P. aeruginosa E. coli A. baumannii None** Respiratory 4/4*** 4/4 2/2 4/4 2/2 1/1  4/10 Urine 9/9*** 1/1 0/1 Wound 1/1 3/3 2/2 Nasal Swab 5/5 3/3 1/1 2/4 **None, Negative culture results or culture detected other organisms Bold-face type indicates antibiotic resistance genes detected by amplicon sequencing ***In one sample, the inventors found a fluoroquinolone-conferring mutation in the gyrA gene.

TABLE 5 False Positives False Positives* Specimen Type K. pneumoniae S. aureus S. pneumoniae P. aeruginosa E. coli A. baumannii Respiratory 1 3 0 0 1 1 Urine 1 Wound Nasal Swab 2 0 0 *Detected by methodology when culture was negative or detected other organisms.

TABLE 6 Identification of Bacterial Species and Antibiotic Resistances in 27 Respiratory Specimen Samples from Subjects with Cystic Fibrosis Bacterial Species Identified in Respiratory Specimen Samples Bacteria Identified Number of Identifications P. aeruginosa 22  E. coli 2 (UPEC) MRSA 15 (9 CC5, SCCmecll) MRSE 11  MSSA 1 S. pneumoniae 2 A. baumannii 2 GBS 5 E. faecalis 2 Other Staphylococcus species 3 P. mirabilis 2 Negative 2 Antibiotic Resistance Antibiotic Resistance Number of Identifications Macrolides 10  Fluoroquinolones 3 Trimethroprim-sulfamethoxazole 5 Clindamycin 1

TABLE 7 Identification of Bacterial Species and Antibiotic Resistances in 24 Respiratory Specimen Samples from Subjects with Chronic Rhinosinusitis Bacterial Species Identified in Respiratory Specimen Samples Bacteria Identified Number of Identifications P. aeruginosa 9 MRSA 7 (1 CC5/SCCmecll, several SCCMeclVa, 1 USA300, 5 SCCmecV) MRSE 19 (several SCCmeclVa) MSSA 5 (3 CC8) E. faecalis 1 E. faecium 1 Other Staphylococcus species 2 P. mirabilis 6 E. aerogenes 2 K. pneumoniae 1 (CG258) Antibiotic Resistance Found Antibiotic Resistance Number of Identifications Aminoglycosides 11  ESBL 9 Macrolides 31  Fluoroquinolones 15  Trimethroprim-sulfamethoxazole 12  Clindamycin 4 Tetracycline 8 Vancomycin 2

TABLE 8 Identification of Bacterial Species and Antibiotic Resistances in 38 Respiratory Specimen Samples from Subjects with Various Respiratory Diseases Bacterial Species Identified in Respiratory Specimen Samples Bacteria Identified Number of Identifications P. aeruginosa 8 MRSA 6 (4 SCCMeclVa, 3 USA300) MRSE 4 (1 SCCmeclVa) MSSA 6 (1 CC5) E. faecalis 8 E. faecium 1 Other Staphylococcus species 8 (2 SCCmeclVa) S. pneumoniae 4 A. baumannii 3 P. mirabilis 1 E. aerogenes 1 E. cloacae 3 K. pneumoniae 4 E. coli 4 K. oxytoca 2 GBS 1 Negative 2 Antibiotic Resistance Found Antibiotic Resistance Number of Identifications Aminoglycosides 1 Macrolides 11  Fluoroquinolones 7 Trimethroprim-sulfamethoxazole 4 Clindamycin 1 Tetracycline 3

TABLE 9 Oligonucleotides of Lineage Identification Assays SEQ ID Target purpose Target ID Assay Sequence NO: Streptococcus M59 M59_UT1 AGAGGAGGAGATAGAGTAGGAGAT 354 pyogenes M59 TACCAGCCAGTATGATAAGAAGAGA 355 Staphylococcus SNP USA300_UT1 GCACGTTGATGACTTCTGACA 356 aureus USA300 GCCCACAAACAATCCAACCTTAC 357 S. aureus CC8 SNP CC8_UT1 TGCCCATAACACATTTGACACTTT 358 (excluding ST239) TTCGGCCACAGCTAAACTCG 359 S. aureus SNP USA3-500_UT1 ACCTTATACGGAACATAGCAGACG 360 USA300/500 TCGATGCGCTTCTATCACTTC 361 S. aureus SNP ArchIber_UT_B+ CGCCAAATGACTCGCATTGT 362 Archaic Iberian GCATGTGCCTTTCCGAARTAAA 363 S. aureus SNP TruIber_UT1 GCGCAACAGGGAAGCAA 364 True Iberian TGCGGATGTCCTATGTCTGAAAG 365 S. aureus ST239 SNP ST239_UT1 CATGACCGCCACTATAACCAGA 366 ATGCAACATTAGCAGGAGGATG 367 S. aureus CC5 SNP CC5_UT1 CTGGCGCTCTCCAGCA 368 TTGCAATTAGTGTGTTAGGTGGTAA 369 E. coli strain ID E. coli H30-Rx H30-Rx-snp200_UT GACACCATGCGTTTTGCTTC 370 TCGTACCGGCAACAATTGAC 371 E. coli H30-Rx H30-Rx-snp264_UT GTGGCGATTTCACGCTGTTA 372 TATCCAGCACGTTCCAGGTG 373 trpA trpA_ST131_O16_UT AAAACCGCGCCGCGTTACCT 374 CCAGAAATCGCGCCCGCATT 375 pabB pabB_ST131_O25b TCCAGCAGGTGCTGGATCGT 376 GCGAAATTTTTCGCCGTACTGT 377 uidA uidA_1_UT CATTACGGCAAAGTGTGGGTCAAT 378 CCATCAGCACGTTATCGAATCCTT 379 uidA uidA_2_UT CGTATCACHGTTTGTGTGAACAA 380 GGATTCACYACTTGCAAAGTCC 381 rfbO16 rfbO16_UT ATACCGACGACGCCGATCTG 382 GGATCATTTATGCTGGTACG 383 rfbO25b rfbO25b_UT ATACCGACGACGCCGATCTG 384 TGCTATTCATTATGCGCAGC 385 K. pneumo MLST rpoB gene KpST-rpoB_UT GGCGAAATGGCWGAGAACCA 386 GAGTCTTCGAAGTTGTAACC 387 gapA KpST-gapA_UT TGAAATATGACTCCACTCACGG 388 CTTCAGAAGCGGCTTTGATGGCTT 389 mdh KpST-mdh_UT CCCAACTCGCTTCAGGTTCAG 390 CCGTTTTTCCCCAGCAGCAG 391 phosphoglucose KpST-pgi_UT GAGAAAAACCTGCCTGTACTGCTGGC 392 isomerase CGCGCCACGCTTTATAGCGGTTAAT 393 phoE KpST-phoE_UT ACCTACCGCAACACCGACTTCTTCGG 394 TGATCAGAACTGGTAGGTGAT 395 infB KpST-infB_UT CTCGCTGCTGGACTATATTCG 396 CGCTTTCAGCTCAAGAACTTC 397 tonB KpST-tonB_UT CTTTATACCTCGGTACATCAGGTT 398 ATTCGCCGGCTGRGCRGAGAG 399 ST258 ID assay/ SNP 3576137-Y ST258_UT_FB ATGGTGGTGCGCCAGTG 400 Kp-species ID GCTGACCGAGACGTTGTC 401 CG258 ID assay CG258_UT_FB ACGGCAGGCGATTTGATTTAACG 402 AGCTGCGTGATCGAGACCTATC 403 E. coli MLST adk EcST-adk_UT TCATCATCTGCACTTTCCGC 404 CCAGATCAGCGCGAACTTCA 405 fumC EcST-fumC_UT TCACAGGTCGCCAGCGCTTC 406 TCCCGGCAGATAAGCTGTGG 407 gyrB EcST-gyrB_UT TCGGCGACACGGATGACGGC 408 GTCCATGTAGGCGTTCAGGG 409 icd EcST-icd_UT ATGGAAAGTAAAGTAGTTGTTCCGGCACA 410 GGACGCAGCAGGATCTGTT 411 mdh EcST-mdh_UT AGCGCGTTCTGTTCAAATGC 412 CAGGTTCAGAACTCTCTCTGT 413 purA EcST-purA_UT TCGGTAACGGTGTTGTGCTG 414 CATACGGTAAGCCACGCAGA 415 recA EcST-recA_UT ACCTTTGTAGCTGTACCACG 416 AGCGTGAAGGTAAAACCTGTG 417 S. aureus MLST arc SaST-arc_UT TTGATTCACCAGCGCGTATTGTC 418 AGGTATCTGCTTCAATCAGCG 419 aro SaST-aro_UT ATCGGAAATCCTATTTCACATTC 420 GGTGTTGTATTAATAACGATATC 421 glp SaST-glp_UT CTAGGAACTGCAATCTTAATCC 422 TGGTAAAATCGCATGTCCAATTC 423 gmk SaST-gmk_UT ATCGTTTTATCGGGACCATC 424 TCATTAACTACAACGTAATCGTA 425 pta SaST-pta_UT GTTAAAATCGTATTACCTGAAGG 426 GACCCTTTTGTTGAAAAGCTTAA 427 tpi SaST-tpi_UT TCGTTCATTCTGAACGTCGTGAA 428 TTTGCACCTTCTAACAATTGTAC 429 yqi SaST-yqi_UT CAGCATACAGGACACCTATTGGC 430 CGTTGAGGAATCGATACTGGAAC 431 

What is claimed is:
 1. A method of detecting and characterizing one or more microorganisms within a sample, the method comprising the steps of: receiving the sample; extracting a template from the sample; performing a multiplex polymerase chain reaction assay comprising the steps of: amplifying a first marker from the template to create a first amplicon, comprising mixing the template with a first oligonucleotide comprising a sequence selected from SEQ ID Nos: 1-49, 54-109; and a second oligonucleotide comprising a sequence selected from SEQ ID Nos: 1-49, 54-109, wherein the first oligonucleotide and the second oligonucleotide independently comprise sequences selected from SEQ ID Nos: 1-49, 54-109 and wherein the first marker is specific for at least a genus of microorganism; amplifying a second marker from the template to create a second amplicon, comprising mixing the template with a third oligonucleotide and a fourth oligonucleotide, wherein the second marker is specific for at least one antibiotic resistance gene; amplifying a third marker from the template to create a third amplicon, comprising mixing the template with a fifth oligonucleotide and a sixth oligonucleotide comprising, wherein the third marker is specific for strain identity and/or lineage of the one or more microorganisms; wherein the multiplex polymerase chain reaction assay is performed within a single reaction vessel; and sequencing the first, second, and third amplicons to detect and characterize the one or more microorganisms.
 2. The method of claim 1, wherein the third and fourth oligonucleotide independently comprise a sequence selected from SEQ ID NOs: 110-298.
 3. The method of claim 1, wherein the fifth and sixth oligonucleotide independently comprise a sequence selected from SEQ ID NOs: 299-431.
 4. The method of claim 1, further comprising adding an index to the first amplicon, second amplicon, and third amplicon using at least one indexing oligonucleotide.
 5. The method of claim 1, wherein at least one of the one or more microorganisms is a pathogenic microorganism selected from the group consisting of: Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp.
 6. The method of claim 1, wherein the template comprises nucleic acids from a subject and the one or more microorganisms and the template comprises DNA.
 7. The method of claim 1, wherein the subject is an animal.
 8. The method of claim 7, wherein the animal is a human.
 9. The method of claim 1, wherein the sample is selected from at least one of a respiratory sample, a nasal swab sample, a urine sample, and a blood sample.
 10. A method of detecting and characterizing one or more microorganisms within a sample, the method comprising the steps of: receiving the sample; extracting a template from the sample; performing a multiplex polymerase chain reaction assay comprising the steps of: amplifying a first marker from the template to create a first amplicon, comprising mixing the template with a first oligonucleotide comprising a sequence selected from SEQ ID Nos: 54-57; and a second oligonucleotide comprising a sequence selected from SEQ ID Nos: 54-57, wherein the first oligonucleotide and the second oligonucleotide independently comprise sequences selected from SEQ ID Nos: 54-57 and wherein the first marker is specific for at least a genus of microorganism; amplifying a second marker from the template to create a second amplicon, comprising mixing the template with a third oligonucleotide and a fourth oligonucleotide, wherein the second marker is specific for at least one antibiotic resistance gene; amplifying a third marker from the template to create a third amplicon, comprising mixing the template with a fifth oligonucleotide and a sixth oligonucleotide, wherein the third marker is specific for strain identity and/or lineage of the one or more microorganisms; wherein the multiplex polymerase chain reaction assay is performed within a single reaction vessel; and sequencing the first, second, and third amplicons to detect and characterize the one or more microorganisms.
 11. The method of claim 10, wherein the third and fourth oligonucleotide independently comprise a sequence selected from SEQ ID NOs: 110-298.
 12. The method of claim 10, wherein the fifth and sixth oligonucleotides independently comprise a sequence selected from SEQ ID NOs:299-431.
 13. The method of claim 10, further comprising adding an index to the first amplicon, second amplicon, and third amplicon using at least one indexing oligonucleotide.
 14. The method of claim 10, wherein the template comprises nucleic acids from a subject and the one or more microorganisms and the template comprises DNA.
 15. The method of claim 10, wherein the subject is an animal.
 16. The method of claim 15, wherein the animal is a human.
 17. The method of claim 10, wherein the sample is selected from at least one of a respiratory sample, a nasal swab sample, a urine sample, and a blood sample.
 18. A method of detecting and characterizing one or more microorganisms within a sample, the method comprising the steps of: extracting a template from the sample; performing a multiplex polymerase chain reaction assay comprising the steps of: amplifying a first marker from the template to create a first amplicon, comprising mixing the template with a first oligonucleotide comprising a sequence selected from SEQ ID Nos: 1-49, 54-109; and a second oligonucleotide comprising a sequence selected from SEQ ID Nos: 1-49, 54-109, wherein the first oligonucleotide and the second oligonucleotide independently comprise sequences selected from SEQ ID Nos: 1-49, 54-109 and wherein the first marker is specific for at least a genus of microorganism; amplifying a second marker from the template to create a second amplicon, comprising mixing the template with a third oligonucleotide and a fourth oligonucleotide, wherein the second marker is specific for at least one antibiotic resistance gene; and amplifying a third marker from the template to create a third amplicon, comprising mixing the template with a fifth oligonucleotide and a sixth oligonucleotide comprising, wherein the third marker is specific for strain identity and/or lineage of the one or more microorganisms; and sequencing the first, second, and third amplicons to detect and characterize the one or more microorganisms.
 19. The method of claim 18, wherein the third and fourth oligonucleotide independently comprise a sequence selected from SEQ ID NOs: 110-298.
 20. The method of claim 18, wherein the fifth and sixth oligonucleotide independently comprise a sequence selected from SEQ ID NOs: 299-431. 